1. Volume 91, Issue 7, Pages 2665-2677 (October 2006)
Spatially and Temporally Synchronized Atomic Force and Total Internal Reflection Fluorescence Microscopy for Imaging and Manipulating Cells and Biomolecules 
Miklós S.Z. Kellermayer, Árpád Karsai, András Kengyel, Attila Nagy, Pasquale Bianco, Tamás Huber, Ágnes Kulcsár, Csaba Niedetzky, Roger Proksch, László Grama 
Biophysical Journal 
Volume 91, Issue 7, Pages (October 2006)
DOI: /biophysj
Copyright © 2006 The Biophysical Society Terms and Conditions

2. Figure 1
Schematics of the epifluorescence optical path of the synchronized TIRF/AFM instrument. (Upper inset) Schematics of wide-field TIRFM combined with AFM. (Lower inset) Schematics of confocal, partial TIRFM (focused TIRFM) combined with AFM.
Biophysical Journal  , DOI: ( /biophysj )
Copyright © 2006 The Biophysical Society Terms and Conditions

3. Figure 2
(a) Image of individual actin filaments bound to an HMM-coated surface acquired with scanning wide-field TIRFM. Scale bar, 10μm. (b) Intensity profile across an actin filament. (c). Intensity profile along the contour of an actin filament (gray) and along an arbitrary line in the background (black). (d) Scanning wide-field TIRFM image of HeLa cells labeled with TRITC-phalloidin. The cells were fixed with paraformaldehyde, then washed and imaged in PBS. Scale bar, 10μm.
Biophysical Journal  , DOI: ( /biophysj )
Copyright © 2006 The Biophysical Society Terms and Conditions

4. Figure 3
Image of cultured HeLa cells acquired with synchronized TIRF-AFM. (a). Height contrast. (b) Amplitude (error) contrast. (c) Phase contrast. (d) TIRF image. Scale bar, 10μm. (e) 3D surface plot of height image colored with fluorescence data. Color bar shows rate meter readings in millivolts, which corresponds to fluorescence intensity. The cells were fixed, labeled with TRITC-phalloidin, washed with PBS and water, then dried with a stream of high-purity N2 gas.
Biophysical Journal  , DOI: ( /biophysj )
Copyright © 2006 The Biophysical Society Terms and Conditions

5. Figure 4
Images of subcortical actin-containing filamentous structures in cultured HeLa cells acquired with synchronized TIRF-AFM. (a) Low-magnification height contrast image. (b) High-magnification height contrast image. (c) Low-magnification amplitude contrast image. (d) High-magnification height contrast image. (e) Low-magnification scanning wide-field TIRFM image. Scale bar, 2μm. (f) High-magnification scanning wide-field TIRFM image. Scale bar, 500nm.
Biophysical Journal  , DOI: ( /biophysj )
Copyright © 2006 The Biophysical Society Terms and Conditions

6. Figure 5
Synchronized TIRF-AFM image of Oregon-Green-488-labeled titin molecules. (a) Height contrast AFM image obtained by scanning in liquid with Olympus BioLever in AC mode. Scale bar, 5μm. (b) Scanning TIRFM image obtained simultaneously with a. (c) AFM image of a titin oligomer adsorbed to mica obtained by scanning in air with Olympus AC160 cantilever. Scale bar, 200nm. (d) 3D surface plot of a colored with the fluorescence information (b).
Biophysical Journal  , DOI: ( /biophysj )
Copyright © 2006 The Biophysical Society Terms and Conditions

7. Figure 6
Dual-color synchronized TIRF-AFM images of pancreas carcinoma cells labeled with TRITC-phalloidin and anti-cytokeratin antibodies. Red and green fluorescence images were acquired in sequential scans. (a) Height contrast image. (b) Amplitude contrast image. (c) Red fluorescence image, corresponding to F-actin distribution. (d) Green fluorescence image, corresponding to cytokeratin distribution. Scale bar, 10μm. (e) 3D surface plot colored with the red fluorescence information. (f) 3D surface plot colored with the green fluorescence information.
Biophysical Journal  , DOI: ( /biophysj )
Copyright © 2006 The Biophysical Society Terms and Conditions

8. Figure 7
Imaging cultured HeLa cells with synchronized focused TIRF-AFM. (a) Height contrast image. White diagonal line marks the region from where synchronized data were plotted. (b) Amplitude contrast image. (c) Focused STIRF-AFM image. Scale bar, 5μm. (d) Spatially correlated height and fluorescence intensity. Subcortical actin filaments (i), edge of cell nucleus (ii), nucleolus (iii), and subcortical actin filaments at the other edge of the cell (iv) are indicated. (e) Testing of photobleaching in sequential scans with focused STIRF-AFM. The acquisition of each scan required 3min. (f) Color density histograms of the focused STIRF-AFM images.
Biophysical Journal  , DOI: ( /biophysj )
Copyright © 2006 The Biophysical Society Terms and Conditions

9. Figure 8
Mechanical manipulation of cells and molecules with synchronized TIRF/AFM. (a) Ablation of a section of a cultured HeLa cell labeled with TRITC-phalloidin. The image labeled “Pre” shows the conditions before mechanical manipulation. White line indicates with arrow the lithographic path traveled by the cantilever tip. The image labeled “Post” shows the effect of mechanical manipulation. The region marked with a star is the section of the cell that has been removed. Scale bar, 10μm. (b) Cutting actin filaments using nanolithographic methods. The image labeled “Pre” shows the conditions before the mechanical manipulation. White lines with arrows indicate the lithographic paths traveled by the cantilever tip. The image labeled “Post” shows the effect of the mechanical manipulation. The regions marked with a star are areas from which a segment of the respective actin filaments were removed. Scale bar, 5μm. (c) Mechanical manipulation of TMRIA-labeled titin preadsorbed to the cantilever tip (Olympus BioLever). (Framed inset) Schematics of the experimental arrangement. (c) (i–iii) Examples of force curves. Black line is data obtained during stretch; gray line is data obtained during relaxation. Sudden changes in fluorescence intensity are marked with asterisk. (d) Mechanical manipulation of TMRIA-labeled titin preadsorbed to the glass coverslip surface. The cantilever was Olympus BioLever. (Framed inset) Schematics of the experimental arrangement. Black line is data obtained during stretch, gray line is data obtained during relaxation. Sudden change in fluorescence intensity, observed in the stretch data, is marked with asterisk. (e) Fluorescence intensity as a function of tip-surface distance and evanescent field depth. (Framed inset) Schematics of the experimental arrangement. Silicon-nitride cantilever Au-coated on backside was used (Veeco Microlever). The number sign (#) indicates the location of tip-surface engagement. (f) Absorption spectrum of the TMRIA-labeled titin sample used in the experiments.
Biophysical Journal  , DOI: ( /biophysj )
Copyright © 2006 The Biophysical Society Terms and Conditions